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Genetic Association of Pulmonary Surfactant Protein Genes, SFTPA1, SFTPA2, SFTPB, SFTPC, and SFTPD With Cystic Fibrosis

Frontiers in immunology, 2018-10, Vol.9, p.2256

2018

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High-throughput DNA methylation profiling using universal bead arrays

Genome Research, 2006-03, Vol.16 (3), p.383-393

2006

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Sex and SP-A2 Dependent NAD(H) Redox Alterations in Mouse Alveolar Macrophages in Response to Ozone Exposure: Potential Implications for COVID-19

Antioxidants, 2020-09, Vol.9 (10), p.915

2020

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NOD2/CARD15 Mutations Correlate With Severe Pouchitis After Ileal Pouch-Anal Anastomosis

Diseases of the colon & rectum, 2010-11, Vol.53 (11), p.1487-1494

2010

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A general model for multilocus epistatic interactions in case-control studies

PloS one, 2010-08, Vol.5 (8), p.e11384-e11384

2010

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Mutations in IRGM Are Associated With More Frequent Need for Surgery in Patients With Ileocolonic Crohnʼs Disease

Diseases of the colon & rectum, 2012-02, Vol.55 (2), p.115-121

2012

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Association of the haem oxygenase-1 gene with inflammatory bowel disease

Swiss medical weekly, 2017-08, Vol.147 (3132), p.w14456

2017

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Genetic Risk Profiling and Gene Signature Modeling to Predict Risk of Complications After IPAA

Diseases of the colon & rectum, 2012-03, Vol.55 (3), p.239-248

2012

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IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants

Pediatric research, 2012-01, Vol.71 (1), p.107-114

2012

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Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis

Human genetics, 2003-11, Vol.113 (6), p.542-550

2003

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NKX2-3 transcriptional regulation of endothelin-1 and VEGF signaling in human intestinal microvascular endothelial cells

PloS one, 2011-05, Vol.6 (5), p.e20454-e20454

2011

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Genes Regulated by Nkx2-3 in Sporadic and Inflammatory Bowel Disease-Associated Colorectal Cancer Cell Lines

Digestive diseases and sciences, 2010-11, Vol.55 (11), p.3171-3180

2010

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Surfactant protein A, an innate immune factor, is expressed in the vaginal mucosa and is present in vaginal lavage fluid

Immunology, 2004-01, Vol.111 (1), p.91-99

2004

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Single nucleotide polymorphisms (SNPs) of TNFSF15 are associated with surgical diverticulitis

Journal of the American College of Surgeons, 2012-09, Vol.215 (3), p.S32-S32

2012

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Genetic Association of Nonsynonymous Variants of the IL23R with Familial and Sporadic Inflammatory Bowel Disease in Women

Digestive diseases and sciences, 2010-03, Vol.55 (3), p.739-746

2010

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Genes regulated by Nkx2-3 in siRNA-mediated knockdown B cells: Implication of endothelin-1 in inflammatory bowel disease

Molecular genetics and metabolism, 2010-05, Vol.100 (1), p.88-95

2010

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DNA methylation markers of surfactant proteins in lung cancer

International journal of oncology, 2007-07, Vol.31 (1), p.181-191

2007

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Optical Redox Imaging of Lonidamine Treatment Response of Melanoma Cells and Xenografts

Molecular imaging and biology, 2019-06, Vol.21 (3), p.426-435

2019

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Novel, non-radioactive, simple and multiplex PCR-cRFLP methods for genotyping human SP-A and SP-D marker alleles

Disease markers, 1999, Vol.15 (4), p.269-281

1999

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Genetic association and epistatic interaction of the interleukin-10 signaling pathway in pediatric inflammatory bowel disease

World journal of gastroenterology : WJG, 2017-07, Vol.23 (27), p.4897-4909

2017

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An SP-B Gene Mutation Responsible for SP-B Deficiency in Fatal Congenital Alveolar Proteinosis: Evidence for a Mutation Hotspot in Exon 4

Molecular genetics and metabolism, 1998-05, Vol.64 (1), p.25-35

1998

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Differential Expression of PGC1α in Intratumor Redox Subpopulations of Breast Cancer

Advances in experimental medicine and biology, 2018, Vol.1072, p.177-181

2018

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Regulation of translation by upstream translation initiation codons of surfactant protein A1 splice variants

American journal of physiology. Lung cellular and molecular physiology, 2015-01, Vol.308 (1), p.L58-L75

2015

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Identification of Disease-Associated DNA Methylation in B Cells from Crohn’s Disease and Ulcerative Colitis Patients

Digestive diseases and sciences, 2012-12, Vol.57 (12), p.3145-3153

2012

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NKX2-3 (NK2 homeobox 3)

Atlas of genetics and cytogenetics in oncology and haematology, 2017-08 (Begum Akman)

2017

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Genetic Association of Pulmonary Surfactant Protein Genes, SFTPA1, SFTPA2, SFTPB, SFTPC, and SFTPD With Cystic Fibrosis

High-throughput DNA methylation profiling using universal bead arrays

Sex and SP-A2 Dependent NAD(H) Redox Alterations in Mouse Alveolar Macrophages in Response to Ozone Exposure: Potential Implications for COVID-19

NOD2/CARD15 Mutations Correlate With Severe Pouchitis After Ileal Pouch-Anal Anastomosis

A general model for multilocus epistatic interactions in case-control studies

Mutations in IRGM Are Associated With More Frequent Need for Surgery in Patients With Ileocolonic Crohnʼs Disease

Association of the haem oxygenase-1 gene with inflammatory bowel disease

Genetic Risk Profiling and Gene Signature Modeling to Predict Risk of Complications After IPAA

IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infants

Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis

NKX2-3 transcriptional regulation of endothelin-1 and VEGF signaling in human intestinal microvascular endothelial cells

Genes Regulated by Nkx2-3 in Sporadic and Inflammatory Bowel Disease-Associated Colorectal Cancer Cell Lines

Surfactant protein A, an innate immune factor, is expressed in the vaginal mucosa and is present in vaginal lavage fluid

Single nucleotide polymorphisms (SNPs) of TNFSF15 are associated with surgical diverticulitis

Genetic Association of Nonsynonymous Variants of the IL23R with Familial and Sporadic Inflammatory Bowel Disease in Women

Genes regulated by Nkx2-3 in siRNA-mediated knockdown B cells: Implication of endothelin-1 in inflammatory bowel disease

DNA methylation markers of surfactant proteins in lung cancer

Optical Redox Imaging of Lonidamine Treatment Response of Melanoma Cells and Xenografts

Novel, non-radioactive, simple and multiplex PCR-cRFLP methods for genotyping human SP-A and SP-D marker alleles

Genetic association and epistatic interaction of the interleukin-10 signaling pathway in pediatric inflammatory bowel disease

An SP-B Gene Mutation Responsible for SP-B Deficiency in Fatal Congenital Alveolar Proteinosis: Evidence for a Mutation Hotspot in Exon 4

Differential Expression of PGC1α in Intratumor Redox Subpopulations of Breast Cancer

Regulation of translation by upstream translation initiation codons of surfactant protein A1 splice variants

Identification of Disease-Associated DNA Methylation in B Cells from Crohn’s Disease and Ulcerative Colitis Patients

NKX2-3 (NK2 homeobox 3)

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